A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3892663



Internal ID18836797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:34450638..34496365hg38UCSC Ensembl
Outerchr15:34426393..34515668hg38UCSC Ensembl
Innerchr15:34742839..34788566hg19UCSC Ensembl
Outerchr15:34718594..34807869hg19UCSC Ensembl
Innerchr15:32530131..32575858hg18UCSC Ensembl
Outerchr15:32505886..32595161hg18UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg3889276
hg1989276
hg1889276
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25789365, essv25785175, essv25800694, essv25797986, essv25797909, essv25801241, essv25800533, essv25779632, essv25786042, essv25796442, essv25792505, essv25796111, essv25797913, essv25779950, essv25798315, essv25798075, essv25792618, essv25780343, essv25796650, essv25796294, essv25796652, essv25796675, essv25779118, essv25798055, essv25794459, essv25781558, essv25782975, essv25784344, essv25786182, essv25794782, essv25798050, essv25779231, essv25793425, essv25798854, essv25787681, essv25797147, essv25801500, essv25786179, essv25778505, essv25800489, essv25780382, essv25797398, essv25796032, essv25800762, essv25787427, essv25783418, essv25795015, essv25792961, essv25780529, essv25800347, essv25793158, essv25785393, essv25791577, essv25782405, essv25782274, essv25799913, essv25791023, essv25800527, essv25792678, essv25800575, essv25796541, essv25796632, essv25796425, essv25785103, essv25781274, essv25797417, essv25790997, essv25800267, essv25800068, essv25796431, essv25797783, essv25778293, essv25781016, essv25797581, essv25797708, essv25795994, essv25796153, essv25796410, essv25778414, essv25782636, essv25794866, essv25778444, essv25799956, essv25800887, essv25786238, essv25788222, essv25786194, essv25796564, essv25786687, essv25797301, essv25786429, essv25796769, essv25800405, essv25785317, essv25782347, essv25797138, essv25797629, essv25801021, essv25781704, essv25787937, essv25797098, essv25789403, essv25796236, essv25779032, essv25800163, essv25792659, essv25798062, essv25797625, essv25781638, essv25782457, essv25800472, essv25795333, essv25794974, essv25800210, essv25793343, essv25797090, essv25778429, essv25800943, essv25798698, essv25796055, essv25783739, essv25797043, essv25797024, essv25800552, essv25792648, essv25797129, essv25796192, essv25780090, essv25797376, essv25792810, essv25780229, essv25796941, essv25787881, essv25780509, essv25786890, essv25796707, essv25786361, essv25799380, essv25786038, essv25784679, essv25788769, essv25782664, essv25797530, essv25797903, essv25786562, essv25800922, essv25796176, essv25798238, essv25800831, essv25781059, essv25784446, essv25780818, essv25796268, essv25796080, essv25783833, essv25786156, essv25784721, essv25785920, essv25786383, essv25797595, essv25779621, essv25796116, essv25798443, essv25801402, essv25784753, essv25786574, essv25783300, essv25796525
Samples
Known GenesGOLGA8A
MethodSNP array
Analysis
PlatformIllumina HumanHap 550
Illumina HumanHap 610
Illumina Human OmniExpress
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3892663
Frequency
Sample Size3017
Observed Gain15
Observed Loss153
Observed Complex0
Frequencyn/a


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